ENST00000322213.9:c.1761G>A
MANE Select
|
ENSP00000323421.3:p.Glu587=
|
|
ENST00000674590.1:c.993G>A
|
ENSP00000502626.1:p.Glu331=
|
|
ENST00000675065.1:n.1113G>A
|
|
|
ENST00000675504.1:c.1695G>A
|
ENSP00000502524.1:p.Glu565=
|
|
ENST00000322213.8:c.1761G>A
|
ENSP00000323421.3:p.Glu587=
|
|
ENST00000375340.10:c.1695G>A
|
ENSP00000364489.7:p.Glu565=
|
|
NM_001281463.1:c.1695G>A , LRG_773t1:c.1695G>A
|
NP_001268392.1:p.Glu565=
|
|
NM_006306.3:c.1761G>A , LRG_773t2:c.1761G>A
|
NP_006297.2:p.Glu587=
|
|
NM_006306.4:c.1761G>A
MANE Select
|
NP_006297.2:p.Glu587=
|
|